Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.
- NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_assertion description "[The methylenetetrahydrofolate reductase gene C677T polymorphism in patients with homozygous sickle cell disease and stroke.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.
- NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_assertion evidence source_evidence_literature NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.
- NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_assertion SIO_000772 10583261 NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.
- NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_assertion wasDerivedFrom befree-2016 NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.
- NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_assertion wasGeneratedBy ECO_0000203 NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.
- befree-2016 importedOn "2016-02-19" NP268907.RAAX1fL5i937fmB4GzFONvMtA3oaar69ryMCiWa80LbLI130_provenance.